The quest for host targets to combat dengue virus infections

被引:26
|
作者
Acosta, Eliana G. [1 ]
Bartenschlager, Ralf [1 ,2 ]
机构
[1] Heidelberg Univ, Dept Infect Dis Mol Virol, Heidelberg, Germany
[2] German Ctr Infect Res DZIF, Partner Site Heidelberg, Heidelberg, Germany
关键词
INHIBITS FLAVIVIRUS REPLICATION; UNFOLDED PROTEIN RESPONSE; HEPATITIS-C VIRUS; VIRAL REPLICATION; NORDIHYDROGUAIARETIC ACID; PYRIMIDINE BIOSYNTHESIS; ENDOPLASMIC-RETICULUM; TRANSPORT INHIBITOR; CHOLESTEROL LEVELS; HEPARAN-SULFATE;
D O I
10.1016/j.coviro.2016.09.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue virus (DENV) is a human threat of increasing importance. Although a tetravalent vaccine has been recently approved, owing to limited efficacy there is still an urgent need for antiviral drugs to prevent or treat DENV infections. Traditionally, antiviral drug discovery has focused on molecules targeting viral factors. However, thus far the identification of direct-acting antiviral drugs with potent DENV pan-serotypic activity has been problematic. An alternative are host-targeting antiviral drugs that hold great promise for broad-spectrum activity. In this review, we summarize cellular factors and pathways required by DENV for efficient replication and in principle suitable for antiviral therapy, including host-directed inhibitors that have even been advanced into clinical trials.
引用
收藏
页码:47 / 54
页数:8
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